{"title":"邻二碘苯/萘苄基体系合成烷基芳醚和二芳醚。","authors":"Cong Xiao, , , Dianfan Liu, , , Xinhao Li, , , Wenjing Zhu, , , Qihui Wang, , , Tingting Yi, , , Xuejun Liu, , , Xiaodong Chen, , , Shilei Zhang*, , and , Yanwei Hu*, ","doi":"10.1021/acs.joc.5c01905","DOIUrl":null,"url":null,"abstract":"<p >We present here the application of <i>o</i>-diiodobenzene/NaH as an efficient benzyne system in reactions with various alcohols and phenols for the synthesis of alkyl aryl ethers and diaryl ethers. Compared to existing protocols for constructing aryl ethers, our new approach not only employs inexpensive and readily available starting materials with simple operation but also enables the preparation of sterically hindered <i>tert</i>-butyl aryl ethers and polyhalogenated diaryl ethers, which pose significant challenges to conventional methods. Additionally, the products retain an <i>ortho</i>-iodine substituent, facilitating further functionalization to access more complex molecular architectures.</p>","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"90 41","pages":"14827–14834"},"PeriodicalIF":3.6000,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"o-Diiodobenzene/NaH Benzyne System Enables the Synthesis of Alkyl Aryl Ethers and Diaryl Ethers\",\"authors\":\"Cong Xiao, , , Dianfan Liu, , , Xinhao Li, , , Wenjing Zhu, , , Qihui Wang, , , Tingting Yi, , , Xuejun Liu, , , Xiaodong Chen, , , Shilei Zhang*, , and , Yanwei Hu*, \",\"doi\":\"10.1021/acs.joc.5c01905\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >We present here the application of <i>o</i>-diiodobenzene/NaH as an efficient benzyne system in reactions with various alcohols and phenols for the synthesis of alkyl aryl ethers and diaryl ethers. Compared to existing protocols for constructing aryl ethers, our new approach not only employs inexpensive and readily available starting materials with simple operation but also enables the preparation of sterically hindered <i>tert</i>-butyl aryl ethers and polyhalogenated diaryl ethers, which pose significant challenges to conventional methods. Additionally, the products retain an <i>ortho</i>-iodine substituent, facilitating further functionalization to access more complex molecular architectures.</p>\",\"PeriodicalId\":57,\"journal\":{\"name\":\"Journal of Organic Chemistry\",\"volume\":\"90 41\",\"pages\":\"14827–14834\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-10-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Organic Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.joc.5c01905\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.joc.5c01905","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
o-Diiodobenzene/NaH Benzyne System Enables the Synthesis of Alkyl Aryl Ethers and Diaryl Ethers
We present here the application of o-diiodobenzene/NaH as an efficient benzyne system in reactions with various alcohols and phenols for the synthesis of alkyl aryl ethers and diaryl ethers. Compared to existing protocols for constructing aryl ethers, our new approach not only employs inexpensive and readily available starting materials with simple operation but also enables the preparation of sterically hindered tert-butyl aryl ethers and polyhalogenated diaryl ethers, which pose significant challenges to conventional methods. Additionally, the products retain an ortho-iodine substituent, facilitating further functionalization to access more complex molecular architectures.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.